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Genetic prediction of male pattern baldness

PLoS genetics, 2017-02, Vol.13 (2), p.e1006594

2017

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Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature

American journal of human genetics, 2011-06, Vol.88 (6), p.788-795

2011

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Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

Nature genetics, 2010-01, Vol.42 (1), p.24-26

2010

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G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

Nature genetics, 2008-03, Vol.40 (3), p.329-334

2008

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Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1

Nature genetics, 2010-02, Vol.42 (2), p.128-131

2010

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Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts

Genetics (Austin), 2014-07, Vol.197 (3), p.1039-1044

2014

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Achalasia: will genetic studies provide insights

Human genetics, 2010-10, Vol.128 (4), p.353-364

2010

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Volition diminishes genetically mediated amygdala hyperreactivity

NeuroImage (Orlando, Fla.), 2010-11, Vol.53 (3), p.943-951

2010

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Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex

American journal of human genetics, 2013-01, Vol.92 (1), p.81-87

2013

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Novel genetic matching methods for handling population stratification in genome-wide association studies

BMC bioinformatics, 2015-03, Vol.16 (1), p.84-84, Article 84

2015

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Susceptibility variants for male-pattern baldness on chromosome 20p11

Nature genetics, 2008-11, Vol.40 (11), p.1279-1281

2008

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Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder

Journal of affective disorders, 2013-04, Vol.146 (3), p.438-440

2013

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Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci

Scientific reports, 2017-01, Vol.7 (1), p.41071-41071, Article 41071

2017

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The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations

Human molecular genetics, 2009-07, Vol.18 (14), p.2719-2727

2009

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Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5′-region are associated with bipolar affective disorder

Human molecular genetics, 2008-01, Vol.17 (1), p.87-97

2008

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Loss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic Disease

Journal of investigative dermatology, 2007-11, Vol.127 (11), p.2539-2543

2007

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Reduced Cortical Thickness is Associated with the Glutamatergic Regulatory Gene Risk Variant DAOA Arg30Lys in Schizophrenia

Neuropsychopharmacology, 2011-07, Vol.36 (8), p.1747-1753

2011

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A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

Human molecular genetics, 2007-03, Vol.16 (6), p.667-677

2007

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The effect of Neuregulin 1 on neural correlates of episodic memory encoding and retrieval

NeuroImage (Orlando, Fla.), 2010-11, Vol.53 (3), p.985-991

2010

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Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma

Nature communications, 2016-01, Vol.7 (1), p.10290-10290, Article 10290

2016

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Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with differences in frontal brain activation in a working memory task in healthy individuals

NeuroImage (Orlando, Fla.), 2008-10, Vol.42 (4), p.1569-1576

2008

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Glutamate receptor delta 1 ( GRID1 ) genetic variation and brain structure in schizophrenia

Journal of psychiatric research, 2012-12, Vol.46 (12), p.1531-1539

2012

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Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder

Neuroscience letters, 2010-06, Vol.478 (1), p.9-13

2010

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G72 and Its Association With Major Depression and Neuroticism in Large Population-Based Groups From Germany

The American journal of psychiatry, 2008-06, Vol.165 (6), p.753-762

2008

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Genetic prediction of male pattern baldness

Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24

Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1

Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts

Achalasia: will genetic studies provide insights

Volition diminishes genetically mediated amygdala hyperreactivity

Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex

Novel genetic matching methods for handling population stratification in genome-wide association studies

Susceptibility variants for male-pattern baldness on chromosome 20p11

Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder

Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci

The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations

Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5′-region are associated with bipolar affective disorder

Loss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic Disease

Reduced Cortical Thickness is Associated with the Glutamatergic Regulatory Gene Risk Variant DAOA Arg30Lys in Schizophrenia

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

The effect of Neuregulin 1 on neural correlates of episodic memory encoding and retrieval

Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma

Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with differences in frontal brain activation in a working memory task in healthy individuals

Glutamate receptor delta 1 ( GRID1 ) genetic variation and brain structure in schizophrenia

Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder

G72 and Its Association With Major Depression and Neuroticism in Large Population-Based Groups From Germany

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